Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4165508
Max Phase: Preclinical
Molecular Formula: C18H14ClFN2O4S2
Molecular Weight: 440.91
Molecule Type: Small molecule
Associated Items:
ID: ALA4165508
Max Phase: Preclinical
Molecular Formula: C18H14ClFN2O4S2
Molecular Weight: 440.91
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: O=S(=O)(Nc1ccccc1NS(=O)(=O)c1cccc(Cl)c1)c1ccc(F)cc1
Standard InChI: InChI=1S/C18H14ClFN2O4S2/c19-13-4-3-5-16(12-13)28(25,26)22-18-7-2-1-6-17(18)21-27(23,24)15-10-8-14(20)9-11-15/h1-12,21-22H
Standard InChI Key: FRJHGVFMXBSCOW-UHFFFAOYSA-N
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 440.91 | Molecular Weight (Monoisotopic): 440.0068 | AlogP: 4.08 | #Rotatable Bonds: 6 |
Polar Surface Area: 92.34 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 7.14 | CX Basic pKa: | CX LogP: 3.70 | CX LogD: 3.16 |
Aromatic Rings: 3 | Heavy Atoms: 28 | QED Weighted: 0.60 | Np Likeness Score: -1.70 |
1. Lorenz DA, Kaur T, Kerk SA, Gallagher EE, Sandoval J, Garner AL.. (2018) Expansion of cat-ELCCA for the Discovery of Small Molecule Inhibitors of the Pre-let-7-Lin28 RNA-Protein Interaction., 9 (6): [PMID:29937975] [10.1021/acsmedchemlett.8b00126] |
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